Molecular cytogenetic characterisation of a mosaic add(12)(p13.3) with an inv dup(3)(q26.31 --> qter) detected in an autistic boy.
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Somatic genome variations in health and diseaseMulticolor FISH methods in current clinical diagnostics.Prenatally diagnosed partial trisomy 3q case with an omphalocele and less severe phenotype.Insertional translocation leading to a 4q13 duplication including the EPHA5 gene in two siblings with attention-deficit hyperactivity disorder.
P2860
Molecular cytogenetic characterisation of a mosaic add(12)(p13.3) with an inv dup(3)(q26.31 --> qter) detected in an autistic boy.
description
2009 nî lūn-bûn
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2009年の論文
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2009年論文
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2009年論文
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2009年論文
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2009年論文
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2009年論文
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2009年论文
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2009年论文
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2009年论文
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name
Molecular cytogenetic characterisation of a mosaic add
@nl
Molecular cytogenetic characte ...... ) detected in an autistic boy.
@en
type
label
Molecular cytogenetic characterisation of a mosaic add
@nl
Molecular cytogenetic characte ...... ) detected in an autistic boy.
@en
prefLabel
Molecular cytogenetic characterisation of a mosaic add
@nl
Molecular cytogenetic characte ...... ) detected in an autistic boy.
@en
P2093
P2860
P50
P356
P1476
Molecular cytogenetic characte ...... r) detected in an autistic boy
@en
P2093
Anja Weise
Joana B Melo
Joris Vermeesch
Liesbeth Backx
Nadezda Kosyakova
P2860
P2888
P356
10.1186/1755-8166-2-16
P577
2009-08-04T00:00:00Z